InChI=1S/C5H8N2O5/c6-5(12)7-2(4(10)11)1-3(8)9/h2H,1H2,(H,8,9)(H,10,11)(H3,6,7,12)/t2-/m0/s1 |
HLKXYZVTANABHZ-REOHCLBHSA-N |
NC(=O)N[C@@H](CC(O)=O)C(O)=O |
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Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
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metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
(via N-carbamoylaspartic acid )
Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
(via N-carbamoylaspartic acid )
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via N-carbamoylaspartic acid )
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View more via ChEBI Ontology
N-carbamoyl-L-aspartic acid
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carbamyl-L-aspartic acid
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ChemIDplus
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Carbamyl-L-aspartic acid
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HMDB
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L-ureidosuccinic acid
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ChemIDplus
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N-(aminocarbonyl)-L-aspartic acid
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ChemIDplus
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N-Carbamoyl-L-aspartate
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KEGG COMPOUND
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N-CARBAMOYL-L-ASPARTATE
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PDBeChem
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N-carbamoyl-S-aspartic acid
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HMDB
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13184-27-5
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CAS Registry Number
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ChemIDplus
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1726860
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Reaxys Registry Number
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Reaxys
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17439666
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PubMed citation
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Europe PMC
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